chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151514188151514196CTCTCTCC6GENIChomozygous127943655
3151514965151514966CT24GENIChomozygous111777670
3151517534151517535AG22GENIChomozygous111777672
3151519183151519183C19GENIChomozygous127943656
3151519994151519995GC18GENIChomozygous111777676
3151520794151520795GA18GENICpossibly homozygous111777678
3151521214151521215CT18GENIChomozygous111777680
3151521853151521854GA17GENIChomozygous111777682
3151522593151522594A18GENICpossibly homozygous127943658
3151523454151523455AG24GENIChomozygous111777684
3151525264151525265GA17GENIChomozygous111777686
3151526739151526740TC19GENIChomozygous111777688
3151526931151526932GA24GENIChomozygous111777690
3151527834151527836CC28GENIChomozygous127943659
3151528785151528786AG15GENIChomozygous111777692
3151530256151530257CT16GENIChomozygous111777694
3151531761151531762TC32GENIChomozygous111777696
3151535190151535191AG31GENIChomozygous111777698
3151541015151541016AG24GENIChomozygous111777700
3151543171151543172AG23GENIChomozygous111777702
3151544558151544559GA25GENIChomozygous111777704
3151525573151525574TG14GENIChomozygous127994361
3151528472151528486GTGTGTGTGTGCGC15GENICheterozygous131839449